Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267607155
TTN
0.923 0.036 2 178782980 missense variant A/G,T snp 2
rs267607490
DES
0.878 0.143 2 219425734 missense variant C/T snp 4
rs267607554 1 156135925 stop gained C/T snp 1
rs267607573 1.000 0.071 1 156134865 stop gained C/T snp 2
rs267607593 1 156134964 missense variant T/C snp 1
rs267607594 0.923 0.107 1 156130745 missense variant T/C snp 1
rs267607618 1.000 0.071 1 156136350 stop gained C/T snp 2
rs267607646 1 156115266 frameshift variant G/GG in-del 1
rs28933090 0.923 0.143 1 156115172 missense variant T/A,G snp 1
rs28933091 0.923 0.143 1 156134474 missense variant C/A,G snp 2
rs28933092 1.000 0.036 1 156134497 missense variant A/G,T snp 2
rs28933093 0.923 0.071 1 156130741 missense variant G/A snp 2
rs368200299 2 178620285 stop gained G/A,T snp 4.9E-06 3.2E-05 1
rs368452607 2 178588700 stop gained G/A,T snp 4.0E-06; 8.0E-06 3.2E-05 1
rs371488302 0.923 0.071 11 47337792 missense variant C/T snp 4.0E-05 2
rs371678190 2 178578066 stop gained G/A,T snp 4.0E-06; 5.6E-05 3.2E-05 1
rs373040154 0.923 0.143 2 178617388 stop gained G/A,T snp 3.2E-05 3
rs377491278 14 23427773 missense variant C/T snp 1.2E-05 1
rs386134243 0.715 0.321 1 156135967 missense variant C/A,T snp 4.0E-06 14
rs387906875 0.923 0.071 10 119670037 stop gained C/T snp 8.0E-06 3
rs397515939 11 47339758 stop gained G/A,C snp 8.0E-06 9.6E-05 1
rs397516089 0.846 0.036 14 23429807 missense variant C/G,T snp 4
rs397516123 14 23427675 missense variant G/A snp 1
rs397516142 1.000 0.071 14 23425357 missense variant C/A,G,T snp 8.0E-06; 1.6E-05 6.4E-05 2
rs397516190 1.000 0.071 14 23419911 inframe deletion TCTC/T in-del 2